Tri-substituted phenyl derivatives and processes for their preparation

ABSTRACT

Compounds of formula (1) ##STR1## are described wherein Y represents a halogen atom or a group --OR 1 , where R 1  is an optionally substituted alkyl group; R 2  represents an optionally substituted cycloalkyl or cycloalkenyl group; R 3  is a monocyclic or bicyclic aryl group optionally containing one or more heteroatoms selected from oxygen or sulphur atoms or a group --N(R 4 )-- where R 4  is a hydrogen atom or an alkyl group; X is --O--, --S--, or --N(R 4 )--, where R 5  is a hydrogen or an alkyl group; with the proviso that when X is --O-- then R 3  is not a 3-cyanamino-6-pyridazinyl or a 3-chloro-6-pyridazinyl group; and the salts, solvates, hydrates and N-oxides thereof. 
     The compounds are selective and potent inhibitors of phosphodiesterase IV and are useful for the prophylaxis and treatment of inflammatory diseases and the alleviation of conditions associated with central nervous malfunction.

This is a division of U.S. application Ser. No. 08/387,551, filed Feb. 13, 1995, now U.S. Pat. No. 5,491,147 which is a continuation of U.S. application Ser. No. 08/141,873, filed Oct. 22, 1993, now abandoned.

FIELD OF THE INVENTION

This invention relates to a novel series of tri-substituted phenyl derivatives, to processes for their preparation, to pharmaceutical compositions containing them, and to their use in medicine.

BACKGROUND TO THE INVENTION

Many hormones and neurotransmitters modulate tissue function by elevating intra-cellular levels of adenosine 3', 5'-cyclic monophosphate (cAMP). The cellular levels of cAMP are regulated by mechanisms which control synthesis and breakdown. The synthesis of cAMP is controlled by adenylyl cyclase which may be directly activated by agents such as forskolin or indirectly activated by the binding of specific agonists to cell surface receptors which are coupled to adenylyl cyclase. The breakdown of cAMP is controlled by a family of phosphodiesterase (PDE) isoenzymes, which also control the breakdown of guanosine 3', 5'-cyclic monophosphate (cGMP). To date, seven members of the family have been described (PDE I-VII) the distribution of which varies from tissue to tissue. This suggests that specific inhibitors of PDE isoenzymes could achieve differential elevation of cAMP in different tissues, for reviews of PDE distribution, structure, function and regulation, see Beavo & Reifsnyder (1990) TIPS, 11: 150-155 and Nicholson et al (1991) TIPS, 12: 19-27!.

There is clear evidence that elevation of cAMP in inflammatory leukocytes leads to inhibition of their activation. Furthermore, elevation of cAMP in airway smooth muscle has a spasmolytic effect. In these tissues, PDE IV plays a major role in the hydrolysis of cAMP. It can be expected, therefore, that selective inhibitors of PDE IV would have therapeutic effects in inflammatory diseases such as asthma, by achieving both anti-inflammatory and bronchodilator effects.

The design of PDE IV inhibitors has met with limited success to date, in that many of the potential PDE IV inhibitors which have been synthesised have lacked potency and/or have been capable of inhibiting more than one type of PDE isoenzyme in a non-selective manner. Lack of a selective action has been a particular problem given the widespread role of cAMP in vivo and what is needed are potent selective PDE IV inhibitors with an inhibitory action against PDE IV and little or no action against other PDE isoenzymes.

A series of 3-cyanamino- and 3-chloro-(4-alkoxyphenyl)pyridazine compounds are described in European Patent Specification No. 393500. Certain of these compounds are claimed to have broncholoytic and anti-inflammatory activities.

SUMMARY OF THE INVENTION

We have now found a novel series of tri-substituted phenyl derivatives, members of which are potent inhibitors of PDE IV at concentrations at which they have little or no inhibitory action on other PDE isoenzymes. These compounds inhibit the isolated PDE IV enzyme and also elevate cAMP in isolated leukocytes. Certain compounds prevent inflammation in the lungs induced by carrageenan, platelet-activating factor (PAF), interleukin-5 (IL-5) or antigen challenge. These compounds also suppress the hyperresponsiveness of airway smooth muscle seen in inflamed lungs. Certain other compounds are also able to modulate central nervous system (CNS) function. The compounds of the invention am therefore of use in medicine, especially in the prophylaxis and treatment of asthma, and for the alleviation of conditions associated with dementia and other CNS malfunctions.

Thus according to one aspect of the invention, we provide a compound of formula (1) ##STR2## wherein Y is a halogen atom or a group --OR¹, where R¹ is an optionally substituted alkyl group;

R² is an optionally substituted cycloalkyl or cycloalkenyl group;

R³ is a monocyclic or bicyclic aryl group optionally containing one or more heteroatoms selected from oxygen or sulphur atoms or a group --N(R⁴)-- where R⁴ is a hydrogen atom or an alkyl group;

X is --O--, --S--, or --N(R⁵)--, where R⁵ is a hydrogen atom or an alkyl group; with the proviso that when X is --O-- then R³ is not a 3-cyanamino-6-pyridazinyl or a 3-chloro-6-pyridazinyl group; and the salts, solvates, hydrates and N-oxides thereof.

In the compounds of formula (1), when Y is a halogen atom it may be for example a fluorine, chlorine, bromine or iodine atom.

When Y in the compounds of formula (1) is a group --OR¹, R¹ may be, for example, an optionally substituted straight or branched alkyl group, for example, an optionally substituted C₁₋₆ alkyl group, (e.g. a C₁₋₃ alkyl group), such as a methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, n-pentyl, i-pentyl, or n-hexyl group. Optional substituents which may be present on R¹ groups include one or more halogen atoms, e.g. fluorine, chlorine, bromine or iodine atoms.

When R² in the compounds of formula (1) is an optionally substituted cycloalkyl or cycloalkenyl group it may be for example a C₃₋₈ cycloalkyl group such as a cyclobutyl, cyclopentyl, or cyclohexyl group or a C₃₋₈ cycloalkenyl group such as a cyclobutenyl, cyclopentenyl or cyclohexenyl group, each cycloalkyl or cycloalkenyl group being optionally substituted by one, two or three substituents selected from halogen atoms, e.g. fluorine, chlorine, bromine or iodine atoms, C₁₋₆ alkoxy e.g. C₁₋₃ alkyl such as methyl or ethyl, hydroxyl or C₁₋₆ alkoxy e.g. C₁₋₃ alkoxy such as methoxy or ethoxy groups.

Monocyclic or bicyclic aryl groups represented by the group R³ in compounds of formula (1) include for example C₆₋₁₂ optionally substituted aryl groups, for example optionally substituted phenyl or 1or 2-naphthyl groups.

When the monocyclic or bicyclic aryl group contains one or more heteroatoms it may be for example a C₃₋₉ optionally substituted heteroaryl group containing for example one, two or three heteroatoms selected from oxygen or sulphur atoms or --N(R⁴)-- groups. Examples is of such groups include pyrrolyl, furanyl, thienyl, imidazolyl, oxazolyl, thiazolyl, pyrazolyl, pyridinyl, e.g. 2-, 3- or 4- pyridinyl, pyrimidinyl e.g. 5-pyrimidinyl, pyridazinyl e.g. 3-pyridazinyl or, 4-pyridazinyl, quinolinyl eg 4-quinolinyl, isoquinolinyl eg 4-isoquinolinyl, 5, 6, 7, 8- tetrahydroquinolinyl and 5, 6, 7, 8- tetrahydroisoquinoquinolinyl. The heteroaryl group may be attached to the remainder of the molecule of formula (1) through any ring carbon or heteroatom as appropriate.

The aryl or heteroaryl groups represented by R³ in compounds of formula (1) may each optionally be substituted by one, two, three or more substituents R⁶ ! selected from halogen atoms, e.g. fluorine, chlorine, bromine or iodine atoms, or C₁₋₆ alkyl, e.g. methyl or ethyl, C₁₋₆ alkoxy, e.g. methoxy or ethoxy, C₂₋₆ alkylenedioxy, e.g. ethylenedioxy, C₅₋₇ cycloalkoxy, e.g. cyclopentoxy, halo C₁₋₆ alkyl, e.g. trifluoromethyl, C₁₋₆ alkylamino, e.g. methylamino or ethylamino, C₁₋₆ alkylthyl, eg methylthio, amino (NH₂), amino C₁₋₆ alkyl, e.g. aminomethyl or aminoethyl, C₁₋₆ dialkylamino, e.g. dimethylamino or diethylamino, nitro, cyano, hydroxyl (OH), carboxyl (CO₂ H), --CO₂ R⁶ where R⁶ is a C₁₋₆ alkyl e.g. methyl or ethyl, C₆₋₁₂ aryl C₁₋₃ alkyl, e.g. benzyl or phenethyl or C₆₋₁₂ aryl, e.g. phenyl group!, C₁₋₆ alkanoyl e.g. acetyl, sulphonyl (--SO₃ H), C₁₋₆ alkyl-sulphonyl, e.g. methylsulphonyl, aminosulphonyl (--SO₂ NH₂), C₁₋₆ alkyl-aminosulphonyl, e.g. methylaminosulphonyl or ethylamino-sulphonyl, C₁₋₆ dialkyaminosulphonyl, e.g. dimethylaminosulphonyl or diethyl-aminosulphonyl, carboxamido (--CONH₂), C₁₋₆ alkylamino-carbonyl, e.g. methylaminocarbonyl or ethylaminocarbonyl, C₁₋₆ dialkyaminocarbonyl, e.g. dimethylaminocarbonyl or diethylaminocarbonyl, sulphonylamino (--NHSO₂ H), C₁₋₆ alkylsulphonylamino, e.g. methylsulphonylamino or ethylsulphonylamino, C₁₋₆ dialkysulphonylamino, e.g. dimethylsulphonylamino or diethylsulphonylamino C₁₋₆ alkanoylamino, e.g. acetylamino, or C₁₋₆ alkanoylamino C₁₋₆ alkyl, e.g. acetylaminomethyl groups.

It will be appreciated that where two or more R⁶ substituents are present, these need not necessarily be the same atoms and/or groups. The R⁶ substituents may be present at any ring carbon atom away from that attached to the rest of the molecule of formula (1). Thus, for example, in phenyl groups represented by R³ any substituent may be present at the 2-, 3-, 4-, 5- or 6- positions relative to the ring carbon atom attached to the remainder of the molecule.

When the groups --N(R⁴)-- or --N(R⁵)-- are present in the compounds of formula (1), R⁴ and R⁵ may each independently be a hydrogen atom or a C₁₋₆ alkyl group such as a methyl or ethyl group.

The presence of certain substituents in the compounds of formula (1) may enable salts of the compounds to be formed. Suitable salts include pharmaceutically acceptable salts, for example acid addition salts derived from inorganic or organic acids, and salts derived from inorganic and organic bases.

Acid addition salts include hydrochlorides, hydrobromides, hydroiodides, p-toluenesulphonates, phosphates, sulphates, acetates, trifluoroacetates, propionates, citrates, maleates, fumarates, malonates, succinates, lactates, oxalates, tartrates and benzoates.

Salts derived from inorganic or organic bases include alkali metal salts such as sodium or potassium salts, alkaline earth metal salts such as magnesium or calcium salts, and organic amine salts such as morpholine, piperidine, dimethylamine or diethylamine salts.

One particular group of compounds of the invention has the formula (1) where R³ is an unsubstituted monocyclic or bicyclic aryl group optionally containing one or more heteroatoms selected from oxygen or sulphur atoms or a group --N(R⁴)--, and Y, R², R³, R⁴ R⁵ and X are as defined for formula (1).

Another group of compounds according to the invention has the formula (1) where R³ is a monosubstituted monocyclic or bicyclic aryl group optionally containing a heteroatom selected from an oxygen or sulphur atom or a group --N(R⁴)--, and Y, R², R³, R⁴, R⁵ and X are as defined for formula (1).

In the compounds of formula (1), the group Y is preferably an --OR¹ group, especially where R¹ is an optionally substituted C₁₋₃ alkyl group, particularly an ethyl group or, especially, a methyl group. Especially useful substituents which may be present on R¹ groups include one, two or three fluorine or chlorine atoms.

The group X in compounds of formula (1) is preferably --O--.

A particularly useful group of compounds of formula (1) has the formula (2): ##STR3## where R² is an optionally substituted cycloalkyl group; R³ is as defined for formula (1) but is not a 3-cyanamino-6- pyridazinyl or a 3-chloro-6-pyridazinyl group; and the salts, solvates, hydrates and N-oxides thereof.

In the compounds of formulae (1) and (2) R² is preferably an optionally substituted cyclopentyl group. In particular, R² is a cyclopentyl group.

Particularly useful R³ groups in compounds of formulae (1) and (2) include substituted phenyl groups, especially 3- and/or 4-substituted phenyl groups and naphthyl groups, especially 1-naphthyl. Particular groups of these types include 3-nitrophenyl, 3-methoxyphenyl, 4-methoxyphenyl, 3,4-dimethoxyphenyl and 3-cyclopentyloxy-4-methoxyphenyl.

Other particularly useful R³ groups in compounds of formulae (1) and (2) include optionally substituted pyridinyl, particularly 3-pyridinyl and 4-pyridinyl, optionally substituted pyrimidinyl, especially 5-pyrimidinyl, and optionally substituted quinolinyl, 5, 6, 7, 8- tetrahydroquinolinyl, isoquinolinyl and 5, 6, 7, 8-tetrahydroisoquinolinyl, especially optionally substituted 3- or 4-quinolinyl, 4-isoquinolinyl and 5, 6, 7, 8-tetrahydroisoquinolin-4-yl. Optional substituents which may be present on these groups include, for example, amino and methyl groups. Particularly useful substituted groups of this type include 2-methylquinolin-4-yl and 1-aminoisoquinolin-4-yl.

A particularly useful group of compounds of the invention has the formula (1), especially the formula (2), wherein R³ is an optionally substituted pyrimidinyl group, especially an optionally substituted 5-pyrimidinyl group.

A further particularly useful group of compounds of the invention has the formula (1), especially the formula (2) wherein R³ is an unsubstituted or monosubstituted pyridinyl group, in particular a 3-pyridinyl, or, especially, a 4-pyridinyl group.

A still further particularly useful group of compounds of the invention has the formula (1), especially the formula (2) wherein R³ is an optionally substituted isoquinolinyl group, in particular an optionally substituted 4-isoquinolinyl group.

Particularly useful compounds according to the invention are:

5-(3-Cyclopentyloxy-4-methoxyphenyl)pyrimidine;

4-(3-Cyclopentyloxy-4-methoxyphenyl)isoquinoline;

4-(3-Cyclopentyloxy-4-methoxyphenyl)pyridine;

2-Cyclopentyloxy-4-(3-cyclopentyloxy-4-methoxyphenyl)anisole;

4-(3-Cyclopentyloxy-4-methoxyphenyl-)-2-methylquinoline;

2-Cyclopentyloxy-4-(3-nitrophenyl)anisole;

4-(3-Cyclopentyloxy-4-methoxyphenyl)quinoline;

2-Cyclopentyloxy-4-(4-nitrophenyl)anisole;

4-(3-Cyclopentyloxy-4-methoxyphenyl)-2,3,5,6-tetrafluoropyridine;

5-Chloro-3-(3-cyclopentyloxy-4-methoxyphenyl)-2,4,6-trifluoropyridine;

5-(3-Cyclopentyloxy-4-methoxyphenyl)pyrimidine-2-carboxamide; and the salts, solvates, hydrates and N-oxides thereof.

Compounds according to the invention are selective and potent inhibitors of PDE IV. The ability of the compounds to act in this way may be simply determined by the tests described in the Examples hereinafter.

The compounds according to the invention are thus of particular use in the prophylaxis and treatment of human diseases where an unwanted inflammatory response or muscular spasm is present and where the elevation of cAMP levels may be expected to prevent or alleviate the inflammation and relax the muscle. Compounds according to the invention are also of particular use in the treatment of conditions associated with CNS malfunction.

Particular uses to which the compounds of the invention may be put include the prophylaxis and treatment of asthma, especially inflamed lung associated with asthma, or in the treatment of inflammatory airway disease, chronic bronchitis, eosinophillic granuloma, psoriasis and other benign and malignant proliferative skin diseases, endotoxic shock, septic shock, ulcerative colitis, Crohn's disease, reperfusion injury of the myocardium and brain, inflammatory arthritis, chronic glomerulonephritis, atopic dermatitis, urticaria, allergic rhinitis, adult respiratory distress syndrome, diabetes insipidus, allergic conjunctivitis and vernal conjunctivitis.

Compounds according to the invention may also elevate cAMP in lymphocytes and thereby suppress unwanted lymphocyte activation in immune-based diseases such as rheumatoid arthritis, rheumatoid spondylitis, transplant rejection and graft versus host disease.

Compounds according to the invention may also be of particular use for the alleviation of conditions associated with dementia and other CNS malfunction for example in senile dementia (e.g. Alzheimer's disease), multiple infarct dementia and dementia caused by other agencies such as by brain tumours and by cerebral trauma.

For the prophylaxis or treatment of disease the compounds according to the invention may be administered as pharmaceutical compositions, and according to a further aspect of the invention we provide a pharmaceutical composition which comprises a compound of formula (1) together with one or more pharmaceutically acceptable carriers, excipients or diluents.

Pharmaceutical compositions according to the invention may take a form suitable for oral, buccal, parenteral, nasal, topical or rectal administration, or a form suitable for administration by inhalation or insufflation.

For oral administration, the pharmaceutical compositions may take the form of, for example, tablets, lozenges or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding agents (e.g. pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.g. lactose, microcrystalline cellulose or calcium hydrogen phosphate); lubricants (e.g. magnesium stearate, talc or silica); disintegrants (e.g. starch or sodium glycollate); or wetting agents (e.g. sodium lauryl sulphate). The tablets may be coated by methods well known in the art. Liquid preparations for oral administration may take the form of, for example, solutions, syrups or suspensions, or they may be presented as a dry product for constitution with water or other suitable vehicle before use. Such liquid preparations may be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents, emulsifying agents, non-aqueous vehicles and preservatives. The preparations may also contain buffer salts, flavouring, colouring and sweetening agents as appropriate.

Preparations for oral administration may be suitably formulated to give controlled release of the active compound.

For buccal administration the compositions may take the form of tablets or lozenges formulated in conventional manner.

The compounds of formula (1) may be formulated for parenteral administration by injection e.g. by bolus injection or continuous infusion. Formulations for injection may be presented in unit dosage form e.g. in glass ampoule or multi dose containers, e.g. glass vials. The compositions for injection may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising, preserving and/or dispersing agents. Alternatively, the active ingredient may be in powder form for constitution with a suitable vehicle, e.g. sterile pyrogen-free water, before use.

In addition to the formulations described above, the compounds of formula (1) may also be formulated as a depot preparation. Such long acting formulations may be administered by implantation or by intramuscular injection.

For nasal administration or administration by inhalation, the compounds for use according to the present invention are conveniently delivered in the form of an aerosol spray presentation for pressurised packs or a nebuliser, with the use of suitable propellant, e.g. dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas or mixture of gases.

The compositions may, if desired, be presented in a pack or dispenser device which may contain one or more unit dosage forms containing the active ingredient. The pack or dispense device may be accompanied by instructions for administration.

The quantity of a compound of the invention required for the prophylaxis or treatment of a particular inflammatory condition will vary depending on the compound chosen, and the condition of the patient to be treated. In general, however, daily dosages may range from around 100 ng/kg to 100 mg/kg, e.g. around 0.01 mg/kg to 40 mg/kg body weight for oral or buccal administration, from around 10 ng/kg to 50 mg/kg body weight for parenteral administration, and around 0.5 mg to around 1000 mg for nasal administration or administration by inhalation or insufflation.

The compounds according to the invention may be prepared by the following processes. The symbols Y, R², R³ and X when used in the formulae below are to be understood to represent those groups described above in relation to formula (1) unless otherwise indicated.

Thus according to a further aspect of the invention, a compound of formula (1) may be prepared by coupling a boronic acid of formula (3) ##STR4## and a compound R³ -L (where L is a leaving group, for example a halogen atom such as a bromine or chlorine atom) in the presence of a complex metal catalyst. Suitable catalysts include heavy metal catalysts, for example palladium catalysts, such as tetrakis(triphenylphosphine) palladium. The reaction may be performed in an inert organic solvent, for example an aromatic hydrocarbon such as toluene or benzene, or an ether such as dimethoxyethane or dioxane, in the presence of a base, e.g. an alkali carbonate such as sodium carbonate, at an elevated temperature, e.g. the reflux temperature. In general, the metal catalyst and reaction conditions may be selected, depending on the nature of the boronic acid of formula (3) and/or the compound R³ -L, from a range of known alternatives for reactions of this type see for example Miyaura, N et al. Synth. Commun. 1981, 11, 513; Thompson, W. J. and Gaudino, J., J. Org. Chem., 1984, 4,9, 5237 and Sharp, M. J. et al, Tetrahedron Lett., 1987, 28, 5093!.

Intermediates R³ -L are either known compounds or may be prepared from known starting materials by methods analogous to those used for the preparation of the known compounds. Thus, for example, where it is desired to obtain a compound R³ -L where L is a halogen atom such as a bromine or chlorine atom and this compound is not readily available, such a compound may be prepared by diazotisation of the corresponding amine using for example a nitrite such as sodium nitrite in an aqueous acid at a low temperature followed by reaction with an appropriate copper (I) halide in an aqueous acid.

Intermediate acids of formula (3) may be prepared by reaction of a halide of formula (4) ##STR5## where Hal is a halogen atom such as a bromine or chlorine atom! by halogen--metal exchange with a base such as n-butyl or t-butyl lithium followed by a borate such as triisopropylborate optionally at a low temperature e.g. around -70° C., in a solvent such as tetrahydrofuran.

Halides of formula (4) wherein X is --O--, --S-- or --N(R⁴)-- may be prepared by alkylation of a corresponding halide of formula (5) ##STR6## using a compound R2Hal where Hal is as just defined! where necessary in the presence of a base such as caesium or potassium carbonate or an alkoxide such as potassium t-butoxide, in a dipolar aprotic solvent such as an amide, e.g. a substituted amide such as dimethylformamide at ambient temperature or above e.g. around 40° C. to 50° C.

Intermediates of formula (5) where X is --O-- may be prepared by oxidation of an aldehyde of formula (6) ##STR7## using an oxidising agent such as 3-chloroperoxybenzoic acid in a halogenated hydrocarbon such as chloroform at a temperature from around 0° C. to room temperature.

Aldehydes of formula (6) and halides of formula (5) where X is --S-- or --N--(R⁴)-- are either known compounds or may be prepared from known starting materials by methods analogous to those used for the preparation of the known compounds.

In another aspect of the invention a compound of formula (1) may be prepared by reaction of a halide of formula (4) with a borane R³ B(Alk)₂ (where Alk is a C₁₋₄ alkyl group such as an ethyl group) or a boronic acid R³ B(OH)₂ using the reagents and conditions described above for the preparation of compounds of formula (1) from acids of formula (2) see for example Ishikura, M et al, Synthesis. 1984, 936!. Intermediate boranes R³ B(Alk)₂ and boronic acids R³ B(OH)₂ for use in this process are either known compounds or may be prepared using methods analogous to those used for the preparation of the known compounds.

In yet another aspect of the invention, a compound of formula (1) may be prepared by alkylation of a compound of formula (7) ##STR8## with a halide R² Hal, as described above for the preparation of compounds of formula (4), or with an alcohol R² OH, and a phosphine, such as triphenylphosphine, and an activator, for example diethyl azodicarboxylate, in the presence of an organic base such as triethylamine in a solvent such as tetrahydrofuran at an elevated temperature, e.g. the reflux temperature see for example Mitsunobu, O., Synthesis, 1981, 1!.

Intermediates of formula (7) may be prepared by reaction of a boronic acid of formula (3) wherein R² is a hydrogen atom with a compound R³ -L as described above for the preparation of compounds of formula (1) from acids of formula (3). In this reaction the group X--R² may need to be in a protected state. Conventional hydroxy, amino or thiol protecting groups may be used in accordance with standard practice see, for example, Green, T. W. in "Protective Groups in Organic Synthesis" John Wiley and Sons, 1981!.

According to a still further aspect of the invention a compound of formula (1) may be prepared by reaction of an intermediate halide of formula (4) by halogen-metal exchange with a base, for example a lithium base such as n-butyl or t-butyl lithium, followed by reaction with a compound R³ H, using for example the reagents and conditions described above for the preparation of Intermediates of formula (3) from Intermediates of formula (4).

Compounds of formula (1) may also be prepared by interconversion of other compounds of formula (1). Thus, for example, a compound of formula (1) where R³ contains an amino (--NH₂) substituent may be prepared from a corresponding compound where R³ contains a nitro group by reduction, using for example hydrogen in the presence of a metal such as platinum of palladium, optionally in the presence of an acid, such as acetic acid. Similar reduction conditions may also be used to convert a compound of formula (1) where R³ is a quinolinyl or isoquinolinyl group to a corresponding compound where R³ is a 5, 6, 7, 8-tetrahydroquinolinyl or 5, 6, 7, 8-tetrahydroisoquinolinyl group.

In another general example, a group represented by R³ in compounds of formula (1) may be substituted by any of the groups R⁵ by an appropriate addition or displacement reaction using the corresponding unsubstituted or substituted compound of formula (1) and a R⁵ containing nucleophile or electrophile. Thus for example to obtain a group R³ in compounds of formula (1) substituted by an amino (--NH₂) group, the corresponding unsubstituted compound may be reacted with an amide such as sodium amide in an inert solvent such as toluene, at an elevated temperature such as the reflux temperature. In another example, to obtain a group R³ in compounds of formula (1) substituted by a cyano group, a corresponding compound containing a displaceable R⁵ substituent, such as an alkylsulphonyl group, may be reacted with a nitrile such as potassium cyanide, at an elevated temperature. Similarly, compounds of formula (1) wherein R³ contains an amino or alkoxy, e.g. methoxy, substituent may be prepared by treatment of a corresponding compound wherein R³ contains a displaceable R⁵ substituent with an alcoholic, e.g. methanolic, ammonia solution followed by separation of the desired amino and alkoxy compounds.

In another example of an interconversion process, a compound of formula (1) wherein R³ contains a --CH₂ NH₂ substituent may be prepared by reduction of a corresponding compound wherein R³ contains a nitrile group, using for example a complex metal hydride such as lithium aluminium hydride in a solvent such as an ether e.g. diethylether.

In a further example, a compound of formula (1) wherein R³ contains an alkanoylamino or alkanolyaminoalkyl substituent may be prepared by acylation of a corresponding compound wherein R³ contains a --NH₂ or alkylamino group by reaction with an acyl halide in the presence of a base, such as a tertiary amine e.g. triethylamine in a solvent such as dichloromethane.

In yet another example of an interconversion process, a compound of formula (1) wherein R³ contains an alkylsulphonyl substituent may be prepared by oxidation of a corresponding compound wherein R³ contains an alkylthio group using for example an oxidising agent such as a peroxy acid, e.g. 3-chloroperoxybenzoic acid, in an inert solvent such as a halogenated hydrocarbon, e.g. dichloromethane, at a low temperature, e.g. below 10° C.

In a still further example of an interconversion process according to the invention, a compound of formula (1) wherein R³ contains a carboxamido (--CONH₂) substituent may be prepared by oxidation of a corresponding compound where R³ contains a cyano substituent, using an oxidising agent, for example hydrogen peroxide and a base such as sodium hydroxide in a solvent such as an alcohol, e.g. ethanol.

N-oxides of compounds of formula (1) may be prepared by oxidation of the corresponding nitrogen base using an oxidising agent such as hydrogen peroxide in the presence of an acid such as acetic acid, at an elevated temperature, for example around 70° C. to 80° C., or a peroxyacid such as 3-chloroperoxybenzoic acid in a solvent such as a halogenated hydrocarbon, e.g. dichloromethane, at e.g. room temperature.

Salts of compounds of formula (1) may be prepared by reaction of a compound of formula (1) with an appropriate acid or base in a suitable solvent using conventional procedures.

DESCRIPTION OF SPECIFIC EMBODIMENTS

The following examples illustrate the invention.

The following abbreviations are used:

    ______________________________________                                         DMF             dimethylformamide                                              THF             tetrahydrofuran                                                DME             dimethoxyethane                                                EtOAc           ethyl acetate                                                  Et.sub.2 O      diethylether                                                   RT              room temperature                                               t.l.c.          thin layer chromatography                                      ______________________________________                                    

INTERMEDIATE 1 5-Bromo-2-methoxyphenol

A solution of 5-bromo-2-methoxybenzaldehyde (100 g, 0.46 mol) in chloroform (250 ml) was cooled with an ice bath and 3-chloroperoxybenzoic acid (50-60% purity) (146 g, 0.51 mol) chloroform (1000 ml) added. The reaction mixture was allowed to warm slowly to room temperature and stirred for 72 h. The white solid was filtered off and the filtrate concentrated in vacuo. The residue was dissolved in ether (200 ml) and washed with 1M sodium sulphite solution (2×200 ml) then sodium hydrogen carbonate half saturated! (3×200 ml). The ether layer was washed with 10% aqueous sodium hydroxide (3×100 ml) and the combined basic extract was acidified with concentrated hydrochloric acid and extracted with Et₂ O (3×100 ml). The combined organic extract was dried (MgSO₄) and florisil (10 g) filtered and the solvent removed under reduced pressure to give the title compound (90 g) as a pale brown solid.

INTERMEDIATE 2 4-Bromo-2-cyclopentyloxyanisole

Intermediate 1 (90 g) was dissolved in DMF (300 ml), and treated with Cs₂ CO₃ (158 g, 490 mmol), and cyclopentylbromide (73 g, 52.5 ml, 490 mmol). After stirring overnight, Cs₂ CO₃ (35 g, 107 mmol), and cyclopentylbromide (12 ml, 16.7 g, 112 mmol) were added and stirring continued for 2 h. A further portion of cyclopentylbromide (10 ml) and Cs₂ CO₃ (14 g) were then added. After stirring for 1 h, the DMF was evaporated in vacuo and the residue diluted with water (200 ml) and extracted with Et₂ O (3×100 ml). The combined organic extract was washed with NaOH solution (5%, 2×100 ml), water (100 ml), then dried (MgSO₄) and the solvent evaporated in vacuo to give a red oil which was distilled (140° C., 0.3 mbar) to afford the title compound (101 g) as a colourless oil Found: C, 53.11; H, 5.53. C₁₂ H₁₅ BrO₂ requires C, 53.15; H, 5.58%.

INTERMEDIATE 3 3-Cyclopentyloxy-4-methoxyphenylboronic acid

To a stirred solution of Intermediate 2 (8.0 g, 29.5 mmol) in dry THF (60 ml), at -70° C. under an argon atmosphere was added n-butyllithium (1.45M, 23.4 ml, 33.9 mmol) over 10 minutes. After stirring for a further 30 minutes triisopropylborate (11.10 g, 13.6 ml, 59 mmol) was added at such a rate that the temperature did not exceed -60° C. The reaction mixture was stirred at -600° C. for 10 mins then the cooling removed and the reaction allowed to warm to room temperature (20 mins). After stirring for 2 h the reaction was quenched with 10% aqueous HCl solution and stirred for 0.5 h. The reaction mixture was extracted with EtOAc (3×40 ml) and the combined organic extract washed with brine (100 ml), dried (MgSO₄) and the solvent removed in vacuo. The resulting white solid was heated to reflux in Et₂ O/hexane 1:3 then cooled to room temperature and the product filtered off. The filtrate was concentrated in vacuo and the residue flash column chromatographed SiO₂ ; EtOAc/hexane, 1:9 (500 ml), then 1:1 (500 ml)! to afford a second crop. Total yield of the title compound was 5.23 g (m.p. 175°-177° C.). δ_(H) (CDCl₃ ; 80 MHz) 1.6-2.1 (8H, br m, (CH₂)₄), 3.90 (3H, s, OMe), 4.89 (1H, br m, OCHCH₂), 6.95 (1H, d, J 8.0 Hz, ArH ortho to OMe), 7.65-7.85 (2H, m, 2×ArH meta to OMe).

INTERMEDIATE 4 5-Bromoisoquinoline

To a cold (0° C.) solution of HBr--H₂ O (48%) (10 ml) in water (30 ml) was added 5-aminoisoquinoline (5 g; 35 mmol) followed by sodium nitrite (2.4 g; 35 mmol) in water (20 ml). The mixture was added to a warm (75° C.) solution of cuprous bromide (5 g; 35 mmol) in HBr--H₂ O (48%) (50 ml) and stirred overnight at 75° C. The reaction mixture was cooled, basified to pH11 with NaOH (5M) and steamed distilled to afford the title compound (1.4 g) as a colourless crystalline solid (mp 65° C.).

INTERMEDIATE 5 2-Methylthiopyrimidine

To a solution of potassium hydroxide (12 g) in methanol (30 ml) was added 2-mercaptopyrimidine (20 g). The mixture was stirred to achieve total solubility before adding methyl iodide (25.36 g) while keeping the temperature of the reaction below 30° C. with an ice-bath cooling. The stirring was maintained for 2 h at RT before removing the solvent in vacuo. The slurry was extracted with Et₂ O (500 ml), filtered and the solution evaporated to afford a pale yellow oil. Filtration through a silica pad (Et₂ O/hexane, 1:1) gave, after evaporation, the title compound (21 g) as a colourless oil. δ_(H) (CDCl₃ ;) 2.55 (3H, s, CH₃), 6.94 (1H, t,pyrimidine H₅), 8.46 (2H, d, J 4.8 Hz, pyrimidine H₄, H₆).

INTERMEDIATE 6 5-Bromo-2-methylthiopyrimidine

A reaction mixture containing Intermediate 5 (10 g), and bromine (12.7 g) in carbon tetrachloride (200 ml) and in 1,2-dichloroethane (100 ml) was heated to gentle reflux for 3 days. The reaction mixture was poured into aqueous sodium sulphite (20%; 100 ml) and stirred until the orange colour had largely disappeared. The pH was adjusted to 7 with 20% NaOH and the aqueous phase extracted with dichloromethane (3×100 ml). The combined organic phase was washed with brine (50 ml), dried (MgSO₄) and evaporated to give an oil. Flash chromatography SiO₂ ; 10% Et₂ O/hexane! gave the title compound as an off-white solid (mp 63°-65° C.).

EXAMPLE 1 a) 5-(3-Cyclopentyloxy-4-methoxyphenyl)pyrimidine hydrochloride

To a stirred solution of tetrakis(triphenylphosphine) palladium 0! (0.59 g, 0.51 mmol) in DME (150 ml) at room temperature under an argon atmosphere was added 5-bromopyrimidine (3.24 g, 20.4 mmol). After stirring for 20 minutes sodium carbonate (2M, 20.4 ml) was added followed by Intermediate 3 (4.0 g, 17 mmol). The mixture was immediately refluxed for 16 h then poured into half saturated NaCl solution (100 ml). EtOAc (50 ml) was added and the organic phase separated. The aqueous portion was extracted with EtOAc (100 ml) and the combined organic extract washed with brine, dried over MgSO₄ and the solvent evaporated in vacuo to yield a clear oil. Flash column chromatography SiO₂ ; Et₂ O/hexane; 1:1 (1000 ml) then 7:3 (1000 ml)! furnished the title compound free base (4.49 g) as a white crystalline solid.

Treatment of the base with ethanolic HCl afforded the title compound as a pale yellow solid m.p. 131°-147° C. (dec)!. Found: C, 62.33; H, 6.29; N, 9.03. C₁₆ H₁₈ N₂ O₂ HCl requires C, 62.64; H, 6.24; N, 9.13%. δ_(H) (CDCl₃ ; 80 MHz) 1.6-2.1 (8H, br m, (CH₂))₄), 3.90 (3H, s, OMe), 4.87 (1H, br m, OCHCH₂), 7.0-7.25 (3H, m, 1×ortho and 2×meta ArH to OMe), 9.23 (2H, s, pyrimidine H₄,H₆), 9.28 (1H, s, pyrimidine H₂), 10.60 (1H, br s, NH).

The following compounds were prepared in a manner similar to the compound of Example 1a).

b) 2-Chloro-5-(3-cyclopentyloxy-4-methoxyphenyl)pyrimidine

From Intermediate 3 (1.04 g) and 5-bromo-2-chloropyridine (1.0 g). Flash column chromatography SiO₂ ; EtOAc/hexane, 1:9 then 2:8 then 2.5:7.5! yielded the title compound (1.02 g) as a white crystalline solid (mp 88°-90° C). Found: C, 63.10; H, 5.62; N, 9.15. C₁₆ H₁₇ CIN₂ O₂ requires C, 63.05; H, 5.62; N, 9.19%.

c) 4-(3-Cyclopentyloxy-4-methoxyphenyl)-2,3,5,6-tetrafluoropyridine

From Intermediate 3 (1.01 g) and 4-bromo-2,3,5-6-tetrafluoropyridine (1.181 g). Column chromatography SiO₂ ; EtOAc! followed by recrystallisation from hexane furnished the title compound (1.184 g)as an off-white powder (mp 115°-116° C.). Found: C, 59.84; H, 4.55; N, 3.81. C₁₇ H₁₅ NO₂ F₄ requires C, 59.83; H, 4.43; N, 4.10%.

d) 5-Chloro-3-(3-cyclopentyloxy-4-methoxyphenyl)-2,4,6-trifluoropyridine

From Intermediate 3 (1.085 g) and 3,5-dichloro-2,4,6-trifluoropyridine (1.13 g). Column chromatography SiO₂ ; dichloromethane! furnished the title compound (1.125 g) as a white flaky powder (mp 100°-102° C.). Found: C, 57.14; H, 4.30; N, 3.83; Cl, 10.05. C₁₇ H₁₅ ClF₃ NO₂ requires C, 57.07; H, 4.23; N, 3.92; N, 3.92; Cl, 9.91%.

e) 5-(3-Cyclopentyloxy-4-methoxyphenyl)-2-methylthio pyrimidine.

From Intermediate 3 (1.04 g) and Intermediate 6 (1.06 g). Flash column chromatography SiO₂ ; Et₂ O/hexane, 1:2) furnished the title compound (550 mg) as a white crystalline solid (mp 84.5°-86.5° C.). Found C, 64.47; H, 6.25; N, 8.74. C₁₇ H₂₀ N₂ O₂ S requires C, 64.55; H, 6.32; N, 8.86%.

f) 1-(3-Cyclopentyloxy-4-methoxyphenyl)naphthalene

From Intermediate 3 (0.50 g) and 1-bromonaphtalene (0.526 g). Column chromatography SiO₂ ; EtOAc/hexane, gradient elution! gave the title compound (0.485 g) as colourless crystals (mp 123°-125° C.). Found C, 82.45; H, 6.96. C₂₂ H₂₂ O₂ requires C, 82.99; H, 6.96.

EXAMPLE 2 4-(3-Cyclopentyloxy-4-methoxyphenyl)isoquinoline

To DME (15 ml) filtered through alumina under nitrogen was added tetrakis(triphenylphosphine) palladium 0! (51 mg, 0.044 mmol) and 4-bromoisoquinoline (304 mg, 1.46 mmol). The reaction mixture was stirred at room temperature for 20 min before adding aqueous sodium carbonate solution (2M, 1.46 ml) and Intermediate 3 (300 mg, 1.27 mmol). The mixture Was immediately heated to reflux. After 16 h the reaction mixture was poured into water (50 ml) and extracted with Et₂ O (3×40 ml). The organic extract was washed with brine (50 ml), dried (MgSO₄), and the solvent removed under reduced pressure. The crude oil was subjected to flash chromatography (Et₂ O/hexane, 2:3 then 3:2) to afford the title compound (396 mg) as a colourless oil, δ_(H) (CDCl₃ ; 80 MHz) 1.6-2.1 (8H, br m, (CH₂)₄), 3.91 (3H, s, OMe), 4.77 (1H, br m, O CHCH₂), 6.99 (3H, s, 1×ortho and 2×meta ArH to OMe), 7.5-7.7 (2H, m, isoquinoline H₆, H₇), 7.85-8.1 (2H, m, isoquinoline H₅, H₈), 8.43 (1H, s, isoquinoline H₃), 9.17 (1H, s, isoquinoline H₁). m/z 319 (M⁺, 30%), 252 (35), 251 (M⁺ -cyclopentyl, 100), 237 (12), 236 (63), 208 (20), and 190 (11 ).

Treatment of the oil with ethereal HCl/ethanol afforded the hydrochloride salt as a pale yellow solid, m.p. 171°-186° C.(dec) (from acetone)!. Found: C, 70.83; H, 6.19; N. 3.82. C₂₁ H₂₁ NO₂.HCl requires C, 70.88; H, 6.23; N, 3.94%.

EXAMPLE 3 a) 4-(3-Cyclopentyloxy-4-methoxyphenyl)pyridine hydrochloride

Tetrakis(triphenylphosphine) palladium 0! (5 mol %, 89 mg) was added to a solution of 4-bromopyridine hydrochloride (1.54 mol, 0.30 g) in DME (filtered through Grade 1 Alumina, 50 ml) and the mixture stirred under dry nitrogen for 15 minutes. Intermediate 3 (0.40 g, 1.69 mmol) was added as a solid followed by sodium carbonate solution (2M, 1.54 ml) and then a further portion of sodium carbonate (0.1 g). The mixture was immediately heated to reflux. After 16 h, the mixture was cooled, diluted with Et₂ O (150 ml) and brine (100 ml), the organic layer was separated, dried (Na₂ SO₄) and concentrated in vacuo to give a brown oil. The oil was subjected to flash chromatography Et₂ O/EtOAc (100:0 to 50:50)! to yield the title compound free base (0.260 g) as a pale yellow solid.

Treatment of the base with ethanolic-ethereal HCl afforded the title compound as a white solid (m.p. 213°-222° C.) (dec). Found: C, 66.39; H. 6.54; N, 4.49. C₁₇ H₁₉ NO₂. HCl requires C, 66.77; H, 6.59; N, 4.58%), δ_(H) (CDCl₃ ; 80 MHz) 1.6-2.1 (8H; br m, (CH₂)₄), 3.92 (3H, s, OMe), 4.85 (1H, br m, OCHCH₂), 6.99 (1H, d, J 8.6 Hz, ArH ortho to OMe), 7.23 (1H, d, J 2.3 Hz, ArH ortho to cyclopentyloxy), 7.38 (1H, dd, J 8.4, 2.3 Hz, ArH para to cyclopentyloxy), 8.01 (2H, d, J 7.0 Hz, pyridine H₃, H₅), 8.75 (2H, d, J 7.0 Hz, pyridine H₂, H₆); m/z 269 (M^(+-HCl), 43%), 202 (67), 201 (M⁺ -HCl-cyclopentyl), 187 (28), 186 (95), 183 (19), 158 (47), 69 (12), 41 (57), and 36 (43).

The following compounds were prepared in a similar manner to the compound of Example 3a):

b) 2-(3-Cyclopentyloxy-4-methoxyphenyl)toluene

From Intermediate 3 (367 mg) and 2-bromotoluene (293 mg) to yield the title compound (241 mg) as a colourless oil. Found: C, 80.67; H, 7.75. C₁₉ H₂₂ O₂ requires C, 80.82; H, 7.85%. m/z 282 (M⁺, 16%), 215 (15), 214 (M⁺ -cyclopentyl, 100), 200 (11), 199 (32), 181 (15), 153 (12), 124 (24), 109 (11) and 28 (27).

c) Methyl 3(3-Cyclopentyloxy-4-methoxyphenyl)benzoate

From Intermediate 3 (430 mg) and methyl 3-bromobenzoate (356 mg) to yield the title compound (300 mg) as a colourless oil, .sup.ν max. (neat) 2960, 1725, 1520, 1450, 1250, 805, 755 cm⁻¹. δ_(H) (CDCl₃ ; 80 MHz) 1.5-2.1 (8H, br m, (CH₂)₄), 3.83 (3H, s, OMe), 3.89 (3H, s, OMe), 4.83 (1H, br m, OCHCH₂), 6.86 (1H, d, J 9 Hz, ArHortho to OMe), 6.9-7.2 (2H, m, 2×ArHmeta to OMe), 7.44 (1H, d, J 7.5 Hz, ArHmeta to CO₂ Me), 7.66 (1H, ca. dt, J 7.5, 1.5 Hz, ArHH para to CO₂ Me), 7.91 (1H, ca. dt, J 7.5, 1.5 Hz, ArH para to aryl), 8.17 (1H, ca. t, J 1.5 Hz, ArH ortho to CO₂ Me and aryl); m/z 326 (M⁺, 10%), 259 (16), 258 (M⁺ -cyclopentyl, 100), 244 (9), 243 (54), 215 (17) and 41 (9).

d) 4-(4-Chlorophenyl)-2-(cyclopentyloxy)anisole

From Intermediate 3 (300 mg) and 4-bromochlorobenzene (292 mg) to yield the title compound (213 mg) as a white solid m.p. 88°-91° C. (from hexane)!. Found: C, 71.74; H, 6.30. C₁₈ H₁₉ ClO₂ requires C, 71.40; H, 6.32%.

e) 2-Cyclopentyloxy-4-(3-methoxyphenyl)anisole

From Intermediate 3 (1.01 g) and 3-bromoanisole (800 mg) to yield the title compound (350 mg) as a white amorphous powder. Found: C, 76.51; H, 7.46. C₁₉ H₂₂ O₃ requires C, 76.48; H, 7.43%) δ_(H) (CDCl₃ ; 80 MHz) 1.5-2.1 (8H, br m (CH₂)₄), 3.83 (3H, s, OMe), 3.85 (3H, s, OMe), 4.81 (1H, br m, OCHCH₂), 6.7-7.4 (7H, m, ArH); m/z 298 (M⁺, 31%), 231 (15), 230 (M⁺ -cyclopentyl 100), 215 (38), 200 (11), 187 (14) and 41 (14).

f) 2-Cyclopentyloxy-4-(3-cyclopentyloxy-4-methoxyphenyl) anisole

From Intermediate 3 and Intermediate 2 to yield the title compound as pale yellow flakes. Found: C, 75.11; H, 7.81. C₂₄ H₃₀ O₄ requires C, 75.36; H, 7.91%.

g) 2-Cyclopentyloxy-4-(4-nitrophenyl)anisole

From Intermediate 3 (300 mg) and 1-bromo-4-nitrobenzene (300 mg) to yield the title compound (400 mg) as yellow needles, m.p. 119°-120° C. (hexane)!. Found: C, 69.09; H, 6.02; N, 4.45. C₁₈ H₁₉ NO₄ requires C, 69.00; H, 6.11; N, 4.47%) δ_(H) (CDCl₃ ; 80 mHz) 1.6-2.1 (8H, m, (CH₂)₄), 3.88 (3H, s, OMe), 4.83 (1H, br m, OCHCH₂), 6.85-7.20 (3H, ArH ortho to OMe and 2×ArH meta to OMe), 7.62 (2H, dm, J ca. 9 Hz, 2×ArH meta to NO₂); 8.22 (2H, dm, J ca. 9 Hz, 2×ArH ortho to NO₂); m/z 313 (M⁺, 5%), 246 (15), 245 (M⁺ -cyclopentyl, 100), 230 (49), 149 (21), and 83 (15).

h) 4-(3-Cyanophenyl)-2(cyclopentyloxy)anisole

From Intermediate 3 (500 mg) and 3-bromobenzonitrile (440 mg) to yield the title compound (610 mg) as a white solid, m.p. 70°-71° C. (hexane-toluene)!. Found: C, 77.72; H, 6.51; N, 4.80. C₁₉ H₁₉ NO₂ requires C, 77.79; H, 6.53; N, 4.77%) 67 _(H) (CDCl₃ ; 80 mHz) 1.6-2.1 (8H, br m, (CH₂)₄), 3.84 (3H, s, OMe), 4.83 (1H, br m, OCHCH₂), 6.85-7.15 (3H, m ArH ortho and 2×ArH meta to OMe), 7.2-7.8 (4H, m, 2×ArH ortho and 2×ArH meta and ArH para to CN); m/z 293 (M⁺, 6%), 226 (16), 225 (M⁺ -cyclopentyl), 211 (9), 210 (60), and 182 (17).

i) 2-(3-Cyclopentyloxy-4-methoxyphenyl)-5)nitropyridine

From Intermediate 3 (300 mg) and 2-bromo-5-nitropyridine (297 mg) to afford the title compound (405 mg) as a pale yellow solid, m.p. 110°-111° C. (diisopropyl ether)!. Found: C, 64.99; H, 5.74; N, 8.89. C₁₇ H₁₈ N₂ O₄ requires C, 64.96; H, 5.74; N, 8.89 δ_(H) (CDCl₃ ; 80 mHz) 1.5-2.1 (8H, br m, (CH₂)₄), 3.90 (3H, s, OMe), 4.90 (1H, br m, OCHCH₂), 6.92 (1H, d, J 8.5 Hz, ArH ortho to OMe), 7.58 (1H, dd, J8.3, 2.0 Hz, ArH para to OMe), 7.70 (1H, d, J 1.4 Hz, ArH ortho to cyclopentyloxy), 7.76 (1H, d, J 8.7 Hz, ArH meta to NO₂), 8.40 (1H, dd, J 8.8, 2.5 Hz, pyridine H₄), 9.37 (1H, d, J 2.5 Hz, pyridine H₂); m/z 314 (M⁺, 14%), 247 (26), 246 (M⁺ -cyclopentyl, 100), 231 (54), 203 (12), 173 (11), 41 (11) 32 (15) and 28 (58).

j) 2-(3-Cyclopentyloxy-4-methoxyphenyl)thiophene

From Intermediate 3 (300 mg) and 2-bromothiophene (238 mg) to afford the title compound (345 mg) as white needles (m.p. 67°-68° C.) (hexane)!. Found: C, 69.96; H, 6.67. C₁₆ H₁₈ O₂ S requires C, 70.04; H, 6.61%; δ_(H) (CDCl₃ ; 80 mHz) 1.5-2.1 (8H, br m, (CH₂)₄), 3.83 (3H, s, OMe), 4.80 (1H, br m, OCHCH₂), 6.80 (1H, d, J 8.7 Hz, ArH ortho to OMe), 6.9-7.2 (5H, m, 2×ArH meta to OMe), and thiopene H₃, H₄, H₅); m/z 274 (M⁺, 24%), 207 (13), 206 (M⁺ -cyclopentyl; 100), 192 (10), 191 (85), 163 (18), and 41 (12).

k) 5-(3-Cyclopentyloxy-4-methoxyphenyl)isoquinoline

From Intermediate 3 (228 mg) and Intermediate 4 (202 mg) to afford the title compound (299 mg) as a white crystalline solid m,p. 115°-116° C. (acetone)!. Found: C, 78.71; H, 6.62; N, 4.30. C₂₁ H₂₁ NO₂ requires C, 78.97; H, 6.63; N, 4.39% δ_(H) (CDCl₃ ; 80 mHz) 1.5-2.1 (8H, br m, (CH₂)₄), 3.90 (3H, s, OMe), 4.75 (1H, br m, OCHCH₂), 6.96 (3H, s, ArH ortho and 2×ArH meta to OMe), 7.55-8.05 (4H, m, isoquinoline H₄, H₆, H₇, H₈), 8.44 (1H, d, J 5.8 Hz, isoquinoline H₃) and 9.23 (1H, s isoquinoline H₁) m/z 319 (M⁺, 24%), 252 (32), 251 (M⁺ -cyclopentyl), 236 (55), 209 (13), 208 (13), 135 (49), and 77(10).

l) 2-(3-Cyclopentyloxy-4-methoxyphenyl)pyridine

From Intermediate 3 (423 mg; 1.79 mmol) and 2-bromopyridine (325 mg; 2.06 mmol), to yield the title compound (0.475 g) as a white crystalline solid m.p. 74°-75° C. (n-hexane)!. δ_(H) (CDCl₃) 1.6-2.1 (8H, br m, (cH₂)₄, 3.87 (3H, S, OMe), 4.91 (1H, br m, OCHCH₂), 6.90 (1H, d, J 8.4 Hz, ArH ortho to OMe), 7.0-7.2 (1H, m, ArH), 7.47 (1H, dd, J 8.4, 2.1 Hz, ArH para to OCp), 7.55-7.7 (3H, m, ArH) and 8.59 (1H, dm, J 4.7 Hz, ArH ortho to pyN); m/z 269 (M⁺, 11%), 202 (15), 201 (M⁺ -Cp, 100), 186 (56), 158 (16), 32 (13), and 28 (53).

Treatment of the title compound with ethereal HCl afforded the hydrochloride salt as a yellow solid m.p. 167°-170° C. (dec) (from ether/ethanol)!. Found: C, 66.67; H, 6.62; N, 4.54. C₁₇ H₁₉ NO₂ HCl requires C, 66.77; H, 6.59; N, 4.58%.

m) 2-(3-Cyclopentyloxy-4-methoxyphenyl)benzonitrile

From Intermediate 3 (1.016 g) and 2-Bromobenzonitrile (0.965 g). Column chromatography SiO₂ ; dichloromethane! furnished the title compound (1.175 g) as colourless oil. Found: C, 77.00; H, 6.52; N. 4.54. C₁₉ H₁₉ NO₂ requires C, 77.52; H, 6.85; N, 4.76%.

EXAMPLE 4 3-(3-Cyclopentyloxy-4-methoxyphenyl)pyridine hydrochloride

A solution of Intermediate 2 (2.812 g, 10.37 mmol) in DME (filtered through Al₂ O₃) (25 ml) was treated with tetrakis(triphenylphosphine) palladium 0! (0.36 g, 0.31 mmol) and stirred at RT for 0.25 h. Diethyl(3-pyridyl)borane (1.50 g, 10.20 mmol) and sodium carbonate 2.2 g, 20.7 mmol) in 10 ml H₂ O! was added and the mixture heated to reflux for 5 h. The mixture was cooled and partitioned between EtOAc (50 ml) and brine (30 ml). The organic layer was separated and combined with a further EtOAc wash (25 ml). The organic extract was washed (brine; 20 ml), dried (Na₂ SO₄), and concentrated in vacuo to yield a yellow oil which was subjected to flash column chromatography (SiO₂ :Et₂ O-hexane;1:1) to give a pale yellow oil (2.14 g). The oil was dissolved in ethanol and treated with Et₂ O-HCl until the title compound just began to precipitate. The mixture was stored at 4° C. for 72 h, then the product was collected by filtration, washed with Et₂ O and dried in vacuo to yield the title compound (1.76 g) as white needles. Found: C, 66.61; H, 6.60; N, 4.47. C₁₇ H₁₉ NO₂. HCl requires C, 66.77; H, 6.59; N, 4.58%). m,/z 269 (M⁺ -HCl, 26%), 202 (34), 201 (M⁺ -HCl-cyclopentyl, 100%), 187 (16), 186 (93), 158 (30).

EXAMPLE 5 4-(3-Cyclopentyloxy-4-methoxyphenyl)-2-methylquinoline hydrochloride hemihydrate

A solution of 4-chloroquinaldine (2.25 g, 12.7 mmol) in dioxane (20 ml) was treated with tetrakis(triphenylphosphine) palladium 0! (440 mg, 0.38 mmol) and stirred at RT for 0.5 h. Intermediate 3 (3.00 g, 12.71 mmol) and Na₂ CO₃ (2.7 g, 25.4 mmol) in ml H₂ O ! was added and the mixture heated to reflux for 18 h. The mixture was cooled and diluted with EtOAc (50 ml) and brine (25 ml). The organic phase was separated and combined with a further EtOAc extract (50 ml). The extract was washed (brine; 25 ml), dried (Na₂ SO₄), and concentrated in vacuo to give a pale brown oil which was flash column chromatographed (SiO₂ ; Et₂ O-hexane; 1:1) to give a colourless oil which crystallised to give a white solid on standing (3.78 g). The solid (0.5 g) was dissolved in ethanoI-HCl then diluted with Et₂ O to the crystallising point. The mixture was allowed to stand in the refrigerator for 48 h, then the supernatant was removed by decantation. The residue was washed with ether then dried in vacuo to afford the title compound as a yellow solid. δ_(H) (CDCl₃ ; 80 MHz) 1.5-2.1 (8H, m (CH₂)₄), 3.19 (3H, s, ArMe), 3.94 (3H, s, OMe), 4.79 (1H, br m, OCHCH₂), 7.01 (1H, s, ArH), 7.05 (2H, s, ArH), 7.44 (1H, s, quinoline H₃), 7.6-8.2 (4H, m, quinoline H₅, H₆, H₇, H₈), 8.99 (1H, d, J 8.0 Hz, NH). m/z 333 (M⁺ -HCl, 12%), 266 (19), 265 (M⁺ -HCl-cyclopentyl, 100%) 250 (19), and 222 (15).

EXAMPLE 6 1-Amino-4-(3-cyclopentyloxy-4-methoxyphenyl)isoquinoline hydrochloride

To a solution of the compound of Example 2 (1.0 g, 3.13 mmol) in dry toluene (20 ml) under nitrogen at room temperature was added a 50% wt suspension of sodium amide in toluene (estimated excess) and this heated to reflux overnight. The reaction mixture was quenched cautiously with water (40 ml) and allowed to stir under nitrogen for 10 mins before pouring into brine (40 ml) and extracting with EtOAc (3×40 ml). The organic extract was washed with brine (60 ml), dried (MgSO₄) and the solvent removed in vacuo. The brown oily residue, was subjected to flash chromatography EtOAc, hexane, 1:3 (500 ml); 1:1 (500 ml) the EtOAc with 2 ml of concentrated NH₃ (1000 ml)! to yield an off-white solid (598 mg) which was dissolved with heating in propan-2-ol and precipitated with diisopropyl ether to afford a pale brown powder (290 mg). The powder was treated with ethereal HCl/ethanol to yield the title compound as an off-white solid. m.p. 253°-257° C. (dec.)!. Found C, 67.63; H, 6.23; N, 7.55. C₂₁ H₂₃ N₂ O₂. HCl requires C, 68.01; H, 6.25; N, 7.55%. m/z 334 (M⁺ -HCl, 46%), 266 (M⁺ -HCl-cyclopentyl, 100).

EXAMPLE 7 2-Cyclopentyloxy-4-(3-nitrophenyl)anisole

i) A mixture of Intermediate 1 (2.50 g) and 3-nitrobenzeneboronic acid (3.10 g) was coupled using the Suzuki conditions exemplified in Example 1 to afford 2-cyclopentyloxy-4-(3-nitrophenyl)phenol (1.0 g) as yellow plates.

ii) 2-Cyclopentyloxy-4-(3-nitrophenyl)phenol (600 mg, 2.45 mmol) was dissolved in DMF (40 ml) and treated with Cs₂ CO₃ (730 mg, 2.24 mmol) and cyclopentyl bromide (0.32 ml, 2.94 mmol). After stirring overnight at RT some of the phenol remained (SiO₂ :t.l.c, CH₂ Cl₂). Cs₂ CO₃ (870 mg, 2.67 mmol) and cyclopentyl bromide (0.32 ml, 2.94 mmol) were added. After stirring at RT for 3 h the phenol had been consumed. The reaction mixture was filtered and concentrated in vacuo. The residue was dissolved in Et₂ O (50 ml), filtered, and concentrated in vacuo to give a yellow solid which was recrystallised from dichloromethane/hexane to afford the title compound (378 mg) as yellow needles. δ_(H) (CDCl₃ ; 80 mHz) 1.5-2.1 (8H, br m, (CH₂)₄), 3.87 (3H, s, OMe), 4.84 (1H, br m, OCHCH₂), 6.91 (1H, d, J9.1 Hz, ArH ortho to OMe), 7.0-7.2 (2H, m, ArH meta to OMe), 7.54 (1H, d, J 7.5 Hz, ArH meta to NO₂), 7.80 (1 H, ca. dt, J ca 7.5, 1.5 Hz, ArH para to NO₂), 8.09 (1H, ca. dt, J ca.8, 1.5 Hz, ArH para to aryl), 8.33 (1H, ca. t, J ca 2 Hz, ArH ortho to NO₂ and aryl); m/z 313 (M⁺, 7%), 246 (17), 245 (M⁺ -cyclopentyl, 100), 230 (41), 202 (8), and 139 (9).

EXAMPLE 8 4-(3-Cyclopentyloxy-4-methoxyphenyl)quinoline

A solution of 4-chloroquinoline (2.08 g; 12.71 mmol) in dioxane (30 ml) was treated with tetrakis (triphenylphosphine)palladium (0) (440 mg; 0.38 mmol) and stirred at room temperature for 0.5 hr. Intermediate 3 (3 g; 12.71 mmol) and Na₂ CO₃ (2.7 g; 25.4 mmol) in H₂ O (12 ml) (ca 2M) were added and the mixture heated to reflux for 18 hr. The reaction mixture was diluted with EtOAc (50 ml) and brine (25 ml) and the organic layer separated. The aqueous layer was re-extracted with EtOAc (50 ml) and the combined organic layer was washed with brine (20 ml), dried (Na₂ SO₄) and concentrated in vacuo to give a pale brown oil (4.91 g). The crude oil was dissolved in Et₂ O -hexane (1:1), and the resulting precipitate collected by filtration, washed with hexane and dried in vacuo to afford the title compound as a white solid. Found C, 78.80; H, 6,56; N, 4.30. C₂₁ H₂₁ NO₂ requires C, 78.97; H, 6.63; N, 4.39%. δ_(H) (CDCl₃) 1.5-2.0 (8H, m, (CH₂)₄), 3.91 (3H, s, OMe), 4.76 (1H, br m, OCHCH₂), 6.99 (3H, s, ArH), 7.27 (1H, D, J 4.7 Hz, quinoline H₃), 7.4-7.7 (2H, m, quinoline H, H), 7.9-8.2 (2H, m, quinoline H, H) and 8.86 (1H, d, J 4.5 Hz, quinoline H₂) .

Dissolution of the title compound (0.5 g) in ethanolic HCl followed by dilution with ether afforded the hydrochloride salt (0.63 g) as a yellow powder. Found C, 70.79; H, 6.14; N, 3.9. C₂₁ H₂₁ NO₂ HCl requires C, 70.88; N, 6.23; N, 3.94%. δ_(H) (CDCl₃) 1.5-2.1 (8H, m, (CH₂)₄), 3.95 (3H, s, OMe), 4.81 (1H, br m, OCHCH₂), 7.09 (3 H, br s, ArH), 7.7-8.3 (5H, m, quinoline H₃, H₅, H₆, H₇, H₈), 8.88 (1H, d, J 8.5 Hz quinoline H₂) and 9.01 (1H, br s, NH)

EXAMPLE 9 4-(3-Cyclopentyloxy-4-methoxyphenyl)-5,6,7,8-tetrahydroisoquinoline

To a solution of the compound of Example 2 (0.5 g; 1.57 mmol) in glacial acetic acid (20 ml) was added platinum (IV) oxide (0.1 g; 0.04 mmol). The reaction mixture was purged with N₂ and stirred for 60 h under a hydrogen atmosphere. The reaction mixture was filtered through celite and the filter washed through with acetic acid (2×10 ml). The filtrate and washings were poured slowly into saturated sodium carbonate solution (100 ml) and extracted with EtOAc (3×60 ml). The combined organic phase was washed with saturated hydrogen carbonate (2×100 ml) and brine (100 ml), dried (MgSO₄) and the solvent removed in vacuo. Purification by column chromatography yielded the title compound (88 mg) δ_(H) (CDCl₃) 1.5-2.1 (12H, br m, OCH(CH₂)₄ +CH₂ (CH₂)₂ CH₂), 2.5-2.9 (4H, br m, CH₂ (CH)₂ CH₂), 3.85 (3H, s, OMe), 4.75 (1H, br m, OCHCH₂), 6.7-6.95 (3H, m, ArH ortho+2×meta to OMe), 8.17 (1H, s, isoquinoline H₁ or H₃) and 8.22 (1H, s, isoquinoline H₁ or H₃).

Treatment of the title compound with ethereal HCl afforded the hydrochloride salt as a yellow crystalline solid (top 189°-191° C.). Found C, 69.66; H, 7.36; N. 3.83. C₂₁ H₂₅ NO₂. HCl requires C, 70.08; H, 7.28; N, 3.89%-m/z 323 (M⁺, 15), 256 (22), 255 (M⁺ -Cp, 100), 240 (M⁺ -Cp-Me, 28), 170 (13), 141 (12), 36 (16), 32 (14), 28 (54).

EXAMPLE 10 5-(3-Cyclopentyloxy-4-methoxyphenyl)pyrimidine-N-oxide

A solution of 5-(3-Cyclopentyloxy-4-methoxyphenyl)pyrimidine (1.37 g) and 3-chloroperoxybenzoic acid (50.60) (1.75 g) in dichloromethane (35 ml) was stirred at RT and the reaction followed by t.l.c. After 5 days, the reaction mixture was partitioned three times between dichloromethane (50 ml) and 10% aqueous Na₂ SO₃ solution (50 ml).

The combined organic phase was washed with 5% aqueous NaOH solution (3×30 ml), brine (30 ml), dried (MgSO₄) and evaporated to afford a tan solid. Flash chromatography SiO₂ ; dichloromethane/EtOAc, 1:9 then dichloromethane/EtOAc/methane, 1:8:1! followed by recrystallisation from EtOAc furnished the title compound (390 g) as a white powder (mp 140°-143° C.). Found=C, 67.03;; H, 6.31; N, 9.81. C₁₆ H₁₈ N₂ O₃ requires C, 67.12; H, 6.34; N, 9.78%.

EXAMPLE 11 a) 3-(3-Cyclopentyloxy-4-methoxyphenyl)pyridazine b) 4-(3-Cyclopentyloxy-4-methoxyphenyl)pyridazine

To a stirred solution of Intermediate 2 (3 g) in dry THF (30 ml) at -70° C. under an argon atmosphere was added n-butyllithium (1.6M in hexanes) (7.95 ml) over 15 min. The reaction mixture was stirred at -70° C. for 15 mins, neat pyridazine (0.96 ml) was then added and the mixture allowed to warm slowly (ca. 1 h) to room temperature. The solution was quenched with 5% aqueous acetic acid solution (5 ml) then partitioned several times between EtOAc and water. The combined organic phase was washed with aqueous NaHCO₃, brine, dried (MgSO₄) then concentrated in vacuo to yield a dark oil (2.8 g). Flash chromatography SiO₂ ; 2% methanol/dichloromethane! gave two fractions containing the two title compounds.

Recrystallisation (from EtOAc/hexane (1:3)) of the first fraction, followed by suspension in hot Et₂ O, cooling and filtration furnished 3-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine (260 mg) as a pale yellow fluffy crystalline solid (mp 112°-114° C.). Found C, 70.99; H, 6.69; N, 10.20. C₁₆ H₁₈ N₂ O₂ requires C, 71.09; H, 6.71; N, 10.36%.

Recrystallisation from EtOAc/hexane (1:5), of the second fraction followed by flash chromatography SiO₂ ; 1% methanol/dichloro methane! then recrystallisation from (EtOAc/hexane, 1:4) furnished 4-(3-Cyclopentyloxy-4-methoxyphenyl) pyridazine (200 mg) as pale yellow needles (mp 100°-102° C.). Found C, 71.16; H, 6.70; N, 10.17. C₁₆ H₁₈ N₂ O₂ requires C, 71.09; H, 6.71; N, 10.36%.

EXAMPLE 12 5-(3-Cyclopentyloxy-4-methoxyphenyl)-2-methylsulphonyl pyrimidine

To a cold (0° C.) solution of the compound of Example 1e (5.82 g) in dichloromethane (100 ml) was added solid 3-chloroperoxybenzoic acid in batches. The temperature was kept below 10° C. and the stirring carried on for 1 h. The precipitate was filtered off and washed with dichloromethane (4×50 ml). The combined organic extract was washed with 10% aqueous Na₂ SO₃ (2×50 ml), saturated aqueous NaHCO₃ (3×50 ml), brine (50 ml), dried (MgSO₄) and evaporated in vacuo. Flash chromatography SiO₂ Et₂ O/hexane, 1:4! followed by recrystallisation from EtOAc furnished the title compound (3.7 g) as a white solid (mp 188°-190° C.). Found C, 58.39; H, 5.76; N, 8.06. C₁₇ H₂₀ N₂ O₄ S requires C, 58.60; H, 5.79; N, 8.04%.

EXAMPLE 13 a) 2-Amino-5-(3-cyclopentyloxy-4-methoxyphenyl)pyrimidine b) 5-(3-Cyclopentyloxy-4-methoxyphenyl)-2methoxy pyrimidine

A solution of the compound of Example 12 (1.0 g) in 2M ammonia and methanol (2.88 ml) in dichloromethane (5 ml) was stirred for 2 days. Ammonia solution (3 ml) was added and the reaction mixture stirred at room temperature for a further 6 days. The solvent was removed in vacuo and the residue purified by flash chromatography SiO₂ ; 2% methanol, dicholoromethane then 5% methanol/dichloromethane! to give two fractions containing the two title compounds.

Concentration in vacuo of the first fraction gave a white crystalline solid which was recrystallised from methanol/hexane to furnish 5-(3-cyclopentyloxy-4-methoxyphenyl)-2-methoxy pyrimidine (380 mg) as a white fluffy solid (mp 91°-93° C.). Found C, 68.05; H, 6.64; H, 9.23. C₁₇ H₂₀ N₂ O₃ requires C, 67.98; H, 6.71; N, 9.33%.

Concentration in vacuo of the second fraction gave a white solid. Recrystallisation from EtOAc/hexane (1:1) furnished 2-amino-5-(3-cyclopentyloxy-4-methoxyphenyl)pyrimidine as a white crystalline powder (50 mg) (mp 167°-169° C.). Found C, 67.25; H, 6.77; N, 14.66. C₁₆ H₁₉ N₃ O₂ requires C, 67.35; H, 6.71; N, 14.73%

EXAMPLE 14 5-(3-Cyclopentyloxy-4-methoxyphenyl)-2-pyrimidine carbonitrile

To a solution of potassium cyanide (205 mg) in dry DMF (10 ml) was added the compound of Example 12 (1.0 g) and the reaction mixture stirred at room temperature for 3 hr then at 50° C. for 2 h. The reaction mixture was poured into a saturated NaHCO₃ solution (2.5 g Na₂ CO₃ in 120 ml ice). The resulting yellow precipitate was filtered off and washed with water. Recrystallisation from EtOAc/hexane (1:2) gave the title compound (575 mg) as yellow needles (mp 121°-123° C.). Found C, 69.15; H, 5.73; N, 14.13. C₁₇ H₁₇ N₃ O₂ requires C, 69.14; H, 5.80; N, 14.23%.

EXAMPLE 15 5-3-Cyclopentyloxy-4-methoxyphenyl)pyrimidine-2-carboxamide

To a stirred mixture of the compound of Example 14 (1.3 g) in ethanol (8 ml) was added hydrogen peroxide (40vols, 15 ml) and 6M aqueous NaOH (6 ml). After 15 min, the reaction mixture was diluted with water (75 ml) and the white solid filtered off. Recrystallisation from acetonitrile furnished the title compound (200 g) as small white plates (mp235°-238° C.). Found C, 65.06; H, 6.09; N, 13.44. C₁₇ H₁₉ N₃ O₃ requires C, 65.16; H, 6.11; N, 13.41%.

The activity and selectivity of compounds according to the invention was demonstrated in the following tests.

1. Isolated Enzyme

The potency and selectivity of the compounds of the invention was determined using a battery of distinct PDE isoenzymes as follows:

i. PDE I, rabbit heart

ii. PDE II, rabbit heart

iii. PDE III, rabbit heart

iv. PDE IV, HL60 cells.

The enzymes were purified to kinetic homogeneity using standard chromatographic techniques.

Phosphodiesterase activity was assayed as follows. The reaction was conducted in 150 μl of standard mixture containing (final concentrations): 50 mM TES-NaOH buffer (pH 7.5), 10 mM MgCl₂, 0.1 μM ³ H!-cAMP and vehicle or various concentrations of the test compounds. The reaction was initiated by addition of enzyme and conducted at 30° C. for between 5 to 30 mins. The reaction was terminated by addition of 50 μl 2% trifluoroacetic acid containing ¹⁴ C!-5' AMP for determining recovery of the product. An aliquot of the sample was then applied to a column of neutral alumina and the ³ H!-cAMP eluted with 10 ml 0.1 TES-NaOH buffer (pH8). The ³ H!-5'-AMP product was eluted with 2 ml 2M NaOH into a scintillation vial containing 10 ml of scintillation cocktail. Recovery of ³ H!-5' AMP was determined using the ¹⁴ C!-5' AMP and all assays were conducted in the linear range of the reaction.

Compounds according to the invention were able to inhibit the action of the PDE IV HL60 enzyme at concentrations at which they had little or no effect on the action of each of the other PDE isoenzymes. Thus, compounds of the Examples have approximate Ki values (Ki PDEIV HL60 at 1 μM) in the nM-μM range, for example the compounds of Examples 2, 4 and 7 have approximate Ki values of 180 nM, 270 nM and 250 nM respectively.

2. The Elevation of cAMP in Leukocytes

The effect of compounds of the invention on intracellular cAMP was investigated using human neutrophils or guinea pig eosinophils. Human neutrophils were separated from peripheral blood, incubated with dihydrocytochalasin B and the test compound for 10 min and then stimulated with FMLP. Guinea pig eosinophils were harvested by peritoneal lavage of animals previously treated with intra-peritoneal injections of human serum. Eosinophils were separated from the peritoneal exudate and incubated with isoprenaline and test compound. With both cell types, suspensions were centrifuged at the end of the incubation, the cell pellets were resuspended in buffer and boiled for 10 min prior to measurement of cAMP by specific radioimmunoassay (DuPont).

The most potent compounds induced a concentration -dependent elevation of cAMP in neutrophils and/or eosinophils at concentrations of 1 nM to 1 μM.

3. Suppression of Leukocyte Function

Compounds of the invention were investigated for their effects on superoxide generation and chemotaxis of human neutrophils. Neutrophils were separated from peripheral blood, incubated with dihydrocytochalasin B for superoxide generation only and test compound prior to stimulation with FMLP. The most potent compounds caused a concentration-dependent inhibition of superoxide generation and chemotaxis at concentrations of 0.1 nM to 1 μM.

4. Relaxation of Constriction Airway Smooth Muscle in vitro

The effects of compounds of the invention on guinea-pig isolated tracheal smooth muscle were investigated. Isolated tracheal rings were suspended in organ baths and immersed in oxygenated Krebs' solution. The smooth muscle was contracted with sub-maximal concentrations of histamine or carbachol prior to the addition of increasing concentrations of test compound to the organ baths. The most potent compounds caused a concentration-dependent reversal of both histamine and carbachol-induced contractions at concentrations of 1 nM to 100 μM. The compounds were generally more potent in reversing histamine-induced tone than carbachol-induced tone.

5. Effect on Cardiac Muscle in vitro

Compounds of the invention have been tested for their effects on isolated cardiac muscle. Right atrial and papillary muscles were dissected out from the hearts of guinea pigs and suspended in organ baths for measuring the rate (chronotropic) of spontaneously beating atria and force (inotropic) of the electrically stimulated papillary muscle. In these preparations, selective PDE IV inhibitors such as rolipram do not have any direct effects whereas selective PDE III inhibitors such as milrinone have positive chronotropic and inotropic effects. The non-specific PDE inhibitor theophylline, which is used in asthma as a bronchodilator, also causes significant cardiovascular changes such as tachycardia. Selective PDE IV inhibitors have advantage over theophylline, therefore, through reduced cardiovascular side effects. The most potent and selective compounds of the invention had no direct effects on the atrial and papillary muscles in vitro at concentrations up to 100 μM but in combination with PDE III inhibitors, these inhibitors showed an enhancement of chronotropic and inotropic activity, typical of selective type IV inhibitors.

6. Anti-allergic Activity in vivo

Compounds of the invention have been tested for effects on an IgE-mediated allergic pulmonary inflammation induced by inhalation of antigen by sensitised guinea pigs. Guinea pigs were initially sensitised to ovalbumin under mild cyclophosphamide-induced immunosuppression, by intraperitoneal injection of antigen in combinations with aluminium hydroxide and pertussis vaccine. Booster doses of antigen were given two and four weeks later and at six weeks, animals were challenged with aerosolised ovalbumin whilst under cover of an intraperitoneally administered anti-histamine agent (mepyramine). After a further 48 h, bronchial alveolar lavages (BAL) were performed and the numbers of eosinophils and other leukocytes in the BAL fluids were counted. The lungs were also removed for histological examination for inflammatory damage. Administration of compounds of the invention (0.1-10 mg/kg i.p.), up to three times during the 48 h following antigen challenge, lead to a significant reduction in the eosinophilia and the accumulation of other inflammatory leukocytes. There was also less inflammatory damage in the lungs of animals treated with compounds of the invention.

7. Effects on Pulmonary Dynamics

Compounds of the invention have been tested for their effects on ozone-induced hyperreactivity of the airways of guinea pigs. Following the inhalation of ozone, guinea pigs become very much more sensitive to the bronchoconstrictor effects of inhaled histamine than naive animals. There is a pronounced shift to the left (10-30 fold) of the dose response curve to histamine and a highly significant increase in the maximum increase in pulmonary resistance. Compounds of the invention administered 1 h prior to ozone by the intraperitoneal (0.01-1 mg/kg) or oral (0.1-10 mg/kg) route caused a dose-dependent inhibition of ozone-induced hyperreactivity.

In general, in our tests above, compounds of the invention have had no observed toxic effects when administered to animals at the doses shown. 

We claim:
 1. A compound of formula (1) ##STR9## wherein: Y is halogen or --OR¹, where R¹ substituted or unsubstituted alkyl;R² is substituted or unsubstituted cycloalkyl or substituted or unsubstituted cycloalkenyl; R³ is pyridinyl, quinolinyl, isoquinolinyl, 5,6,7,8-tetrahydroquinolinyl or 5,6,7,8-tetrahydroisoquinolinyl; wherein each of said R³ groups is independently substituted or unsubstituted; and X is --O--, --S--, or --N(R⁵)--, where R⁵ is hydrogen or alkyl; or a salt, solvate, or N-oxide thereof;with the proviso that when R³ is substituted pyridinyl, said R³ substituent is selected from halo, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₂₋₆ alkylenedioxy, C₅₋₇ cycloalkoxy, haloC₁₋₆ alkyl, C₁₋₆ alkylamino, C₁₋₆ alkylthio, amino (NH₂), amino C₁₋₆ alkyl, C₁₋₆ dialkyamino, nitro, cyano, hydroxyl, carboxyl (--CO₂ H) and carboxyl esterified by C₁₋₆ alkyl, C₆₋₁₂ arylC₁₋₃ alkyl or C₆₋₁₂ aryl, C₁₋₆ alkanoyl (--C(═O)Alk¹), sulphonyl (--SO₃ H), C₁₋₆ alkylsulphonyl (--SO₂ Alk¹), aminosulphonyl (--SO₂ NH₂), C₁₋₆ alkylaminosulphonyl (--SO₂ NHAlk¹), C₁₋₆ dialkylaminosulphonyl (--SO₂ N(Alk¹)₂), carboxamido (--CONH₂), C₁₋₆ alkylaminocarbonyl (--CONHAlk¹), C₁₋₆ dialkyaminocarbonyl (--CON(Alk¹)₂), sulphonylamino (--NHSO₂ H), C₁₋₆ alkylsulphonylamino (--NHSO₂ Alk¹), C₁₋₆ dialkysulphonylamino (--NSO₂ (Alk¹)₂), C₁₋₆ alkanoylamino (--NHC(═O)Alk¹) and C₁₋₆ alkanoylamino C₁₋₆ alkyl (--N(Alk¹)C(═O)Alk¹), where Alk¹ is straight or branched C₁₋₆ alkyl.
 2. A compound of formula (2) ##STR10## wherein: R² is substituted or unsubstituted cycloalkyl; andR³ is pyridinyl, quinolinyl, isoquinolinyl, 5,6,7,8-tetrahydroquinolinyl or 5,6,7,8-tetrahydroisoquinolinyl; wherein each of said R³ groups is independently substituted or substituted; or a salt, solvate, hydrate or N-oxide thereof; with the proviso that when R³ is substituted pyridinyl, said R³ substituent is selected from halo, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₂₋₆ alkylenedioxy, C₅₋₇ cycloalkoxy, haloC₁₋₆ alkyl, C₁₋₆ alkylamino, C₁₋₆ alkylthio, amino (NH₂), aminoC₁₋₆ alkyl, C₁₋₆ dialkyamino, nitro, cyano, hydroxyl, carboxyl (--CO₂ H) and carboxyl esterified by C₁₋₆ alkyl, C₆₋₁₂ aryl C₁₋₃ alkyl or C₆₋₁₂ aryl, C₁₋₆ alkanoyl (--C(═O)Alk¹), sulphonyl (--SO₃ H), C₁₋₆ alkylsulphonyl (--SO₂ Alk¹), aminosulphonyl (--SO₂ NH₂), C₁₋₆ alkylaminosulphonyl (--SO₂ NHAlk¹), C₁₋₆ dialkylaminosulphonyl (--SO₂ N(Alk¹)₂), carboxamido (--CONH₂), C₁₋₆ alkylaminocarbonyl (--CONHAlk¹), C₁₋₆ dialkyaminocarbonyl (--CON(Alk¹)₂), sulphonylamino (--NHSO₂ H), C₁₋₆ alkylsulphonylamino (--NHSO₂ Alk¹), C₁₋₆ dialkylsulphonylamino (--NSO₂ (Alk¹)₂), C₁₋₆ alkanoylamino (--NHC(═O)Alk¹) and C₁₋₆ alkanoylaminoC₁₋₆ alkyl (--N(Alk¹)C(═O)Alk¹), where Alk¹ is straight or branched C₁₋₆ alkyl.
 3. A compound selected from the group consisting of:4-(3-cyclopentyloxy-4-methoxyphenyl)isoquinoline; 4-(3-cyclopentyloxy-4-methoxyphenyl)pyridine; 4-(3-cyclopentyloxy-4-methoxyphenyl)-2-methylquinoline; 4-(3-cyclopentyloxy-4-methoxyphenyl)quinoline; 4-(3-cyclopentyloxy-4-methoxyphenyl)-2,3,5,6-tetrafluoropyridine; and 5-chloro-3-(3-cyclopentyloxy-4-methoxyphenyl)-2,4,6-trifluoropyridine; or a salt, solvate, hydrate and N-oxide thereof.
 4. A compound according to claim 3 which is 4-(3-cyclopentyloxy-4-methoxyphenyl)isoquinoline.
 5. A compound according to claim 3 which is 4-(3-cyclopentyloxy-4-methoxyphenyl)quinoline.
 6. A pharmaceutical composition comprising a compound of formula (1) ##STR11## wherein: Y is halogen or --OR¹, where R¹ is substituted or unsubstituted alkyl;R² is substituted or unsubstituted cycloalkyl or substituted or unsubstituted cycloalkenyl; R³ is pyridinyl, quinolinyl, isoquinolinyl, 5,6,7,8-tetrahydroquinolinyl or 5,6,7,8-tetrahydroisoquinolinyl; wherein each of said R³ groups is independently substituted or substituted; and X is --O--, --S--, or --N(R⁵)--, where R⁵ is hydrogen or alkyl; or a salt, solvate, hydrate or N-oxide thereof; together with one or more pharmaceutically acceptable carriers, excipients or diluents;with the proviso that when R³ is substituent pyridinyl, said R³ substituent is selected from halo, C₁₋₆ alkyl, C₁₋₆ alkoxy, C₂₋₆ alkylenedioxy, C₅₋₇ cycloalkoxy, haloC₁₋₆ alkyl, C₁₋₆ alkylamino, C₁₋₆ alkylthio, amino (NH₂), aminoC₁₋₆ alkyl, C₁₋₆ dialkyamino, nitro, cyano, hydroxyl, carboxyl (--CO₂ H) and carboxyl esterified by C₁₋₆ alkyl, C₆₋₁₂ arylC₁₋₃ alkyl or C₆₋₁₂ aryl, C₁₋₆ alkanoyl (--C(═O)Alk¹), sulphonyl (--SO₃ H), C₁₋₆ alkylsulphonyl (--SO₂ Alk¹), aminosulphonyl (--SO₂ NH₂), C₁₋₆ alkylaminosulphonyl (--SO₂ NHAlk¹), C₁₋₆ dialkyaminosulphonyl (--SO₂ N(Alk¹)₂), carboxamido (--CONH₂), C₁₋₆ alkylaminocarbonyl (--CONHAlk¹), C₁₋₆ dialkyaminocarbonyl (--CON(Alk¹)₂), sulphonylamino (--NHSO₂ H), C₁₋₆ alkylsulphonylamino (--NHSO₂ Alk¹), C₁₋₆ dialkysulphonylamino (--NSO₂ (Alk¹)₂), C₁₋₆ alkanoylamino (--NHC(═O)Alk¹) and C₁₋₆ alkanoylaminoC₁₋₆ alkyl (--N(Alk¹)C(═O)Alk¹), where Alk¹ is straight or branched C₁₋₆ alkyl.
 7. A pharmaceutical composition comprising, together with one or more pharmaceutically acceptable carriers, excipients or diluents, a compound according to claim
 4. 8. A pharmaceutical composition comprising, together with one or more pharmaceutically acceptable carriers, excipients or diluents, a compound according to claim
 5. 9. A method for preventing or treating an inflammatory disease in a patient comprising administering to said patient an effective amount of a composition according to claim
 7. 10. A method for preventing or treating an inflammatory disease in a patient comprising administering to said patient an effective amount of a composition according to claim
 8. 11. A compound according to claim 1 wherein X is --O--.
 12. A compound according to claim 1 wherein Y is --OR¹, where R¹ is substituted or unsubstituted alkyl.
 13. A compound according to claim 1 wherein R² is substituted or unsubstituted cycloalkyl.
 14. A compound according to claim 1 wherein said R¹ substituent is halogen.
 15. A compound according to claim 1 wherein said R² substituent is halogen, hydroxyl, C₁₋₆ alkyl or C₁₋₆ alkoxy.
 16. A compound according to claim 2 wherein R² is cyclopentyl.
 17. A compound according to claim 2 wherein R³ is substituted or unsubstituted 3- or 4- pyridinyl, substituted or unsubstituted 3- or 4-quinolinyl, or substituted or unsubstituted 4-isoquinolinyl.
 18. A compound of formula (8) ##STR12## wherein: R⁸ is substituted or unsubstituted cyclopentyl; andR⁹ is substituted or unsubstituted 3-pyridinyl, substituted or unsubstituted 4-pyridinyl, substituted or unsubstituted 4-isoquinolinyl, substituted or unsubstituted 3-quinolinyl, substituted or unsubstituted 4-quinolinyl, or substituted or unsubstituted 5,6,7,8-tetrahydroisoquinolin-4-yl; or a salt, solvate, hydrate or N-oxide thereof;with the proviso that when R⁹ is substituted pyridinyl, said R⁹ substituent is selected from halo, C₁₋₆ alkyl, C₁ ulcus, C₂₋₆ alkylenedioxy, C₅₋₇ cycloalkoxy, halo C₁₋₆ alkyl, C₁₋₆ alkylamino, C₁₋₆ alkylthio, amino (NH₂), aminoC₁₋₆ alkyl, C₁₋₆ dialkyamino, nitro, cyano, hydroxyl, carboxyl (--CO₂ H) and carboxyl esterified by C₁₋₆ alkyl, C₆₋₁₂ arylC₁₋₃ alkyl or C₆₋₁₂ aryl, C₁₋₆ alkanoyl (--C(═O)Alk¹), sulphonyl (--SO₃ H), C₁₋₆ alkylsulphonyl (--SO₂ Alk¹), aminosulphonyl (--SO₂ NH₂), C₁₋₆ alkylaminosulphonyl (--SO₂ NHAlk¹), C₁₋₆ dialkyaminosulphonyl (--SO₂ N(Alk¹)₂), carboxamido (--CONH₂), C₁₋₆ alkylaminocarbonyl (--(CONHAlk¹), C₁₋₆ dialkyaminocarbonyl (--CON(Alk¹)₂), sulphonylamino (--NHSO₂ H), C₁₋₆ alkylsulphonylamino (--NHSO₂ Alk¹), C₁₋₆ dialkysulphonylamino (--NSO₂ (Alk¹)₂), C₁₋₆ alkanoylamino (--NHC(═O)Alk¹) and C₁₋₆ alkanoylaminoC₁₋₆ alkyl (--N(Alk¹)C(═)Alk¹), where Alk¹ is straight or branched C₁₋₆ alkyl.
 19. A compound of claim 18 wherein R⁹ is substituted or unsubstituted 3-pyridinyl or substituted or unsubstituted 4-pyridinyl.
 20. A compound of claim 18 wherein R⁹ is substituted or unsubstituted 4-isoquinolinyl.
 21. A compound of claim 18 wherein R⁹ is substituted or unsubstituted 4-quinolinyl.
 22. A method for preventing or treating an inflammatory disease in a patient comprising administering to said patient, in combination with a pharmaceutically acceptable carrier, a selective inhibitor of a phosphodiesterase (PDE) IV isoenzyme in an amount sufficient to elevate intracellular levels of adenosine 3',5'-cyclic monophosphate (cAMP), said inhibitor comprising a compound of the formula: ##STR13## wherein: Y is halogen or --OR¹, where R¹ is substituted or unsubstituted alkyl;R² is substituted or unsubstituted cycloalkyl or substituted or unsubstituted cycloakyl; R³ is pyridinyl, quinolinyl, isoquinolinyl, 5,6,7,8-tetrahydroquinolinyl or 5,6,7,8-tetrahydroisoquinolinyl, wherein each of said R³ groups is independently substituted or substituted; and X is --O--, --S--, or --N(R⁵)--; where R⁵ is hydrogen or alkyl; or a salt , solvate, hydrate or N-oxide thereof;with the proviso that when R³ is substituted pyridinyl, said R³ substituent is selected from halo, C₁₋₆ alkyl, C₁ ulcus, C₂₋₆ alkylenedioxy, C₅₋₇ cycloalkoxy, haloC₁₋₆ alkyl, C₁₋₆ alkylamino, C₁₋₆ alkylthio, amino (NH₂), aminoC₁₋₆ alkyl, C₁₋₆ dialkyamino, nitro, cyano, hydroxyl, carboxyl (--CO₂)H) and carboxyl esterified by C₁₋₆ alkyl, C₆₋₁₂ arylC₁₋₃ alkyl or C₆₋₁₂ aryl, C₁₋₆ alkanoyl (--C(═O)Alk¹), sulphonyl (--SO₃ H), C₁₋₆ alkylsulphonyl (--SO₂ Alk¹), aminosulphonyl (--SO₂ NH₂), C₁₋₆ alkylaminosulphonyl (--SO₂ NHAlk¹), C₁₋₆ dialkyaminosulphonyl (--SO₂ N(Alk¹)₂), carboxamido (--CONH₂), C₁₋₆ alkylaminocarbonyl (--CONHAlk¹), C₁₋₆ dialkyaminocarbonyl (--CON(Alk¹)₂), sulphonylamino (--NHSO₂ H), C₁₋₆ alkylsulphonylamino (--NHSO₂ Alk¹), C₁₋₆ dialkysulphonylamino (--NSO₂ (Alk¹)₂), C₁₋₆ alkanoylamino (--NHC(═O)Alk¹) and C₁₋₆ alkanoylaminoC₁₋₆ alkyl (--N(Alk¹)C(═O)Alk¹), where Alk¹ is straight or branched C₁₋₆ alkyl.
 23. A method according to claim 22 wherein the inflammatory disease comprises asthma.
 24. A method according to claim 22 wherein the inflammatory disease is selected from the group consisting of inflammatory airway disease, chronic bronchitis, eosinophilic granuloma, inflammatory arthritis, atopic dermatitis, urticaria, allergic rhinitis, adult respiratory distress syndrome and allergic conjunctivitis. 